A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113377



Internal ID21296643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:3472725..3477516hg38UCSC Ensembl
Innerchr9:3472725..3477516hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg384792
hg194792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14088861
Samplessample409
Known GenesRFX3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113377
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer